US5000743A

Movatterモバイル変換

Info

Publication number: US5000743A
Application number: US07/284,843
Authority: US
Inventors: Piyush V. Patel
Original assignee: Individual
Current assignee: Individual
Priority date: 1987-02-27
Filing date: 1988-12-13
Publication date: 1991-03-19
Anticipated expiration: 2008-03-19

Abstract

Description

This is a continuation of Application No. 07/019,688 filed on Feb. 27, 1987, now U.S. Pat. No. 4,832,020.

TECHNICAL FIELD

This invention relates in general to medical equipment and procedures. In particular, the invention relates to a catheter assembly and a method of using the catheter assembly to perform a medical procedure known as percutaneous transluminal coronary angioplasty.

BACKGROUND AND SUMMARY OF THE INVENTION

The purpose of percutaneous transluminal coronary angioplasty is to open a coronary artery which has become partially blocked by a stenotic lesion. A stenotic lesion is an abnormal narrowing of an artery due to injury or disease.

The procedure involves the introduction of a catheter system into the heart, by way of the femoral artery, under local anesthesia. The catheter system includes a guiding catheter and a dilating catheter. The end of the guiding catheter is inserted into the opening of the coronary artery.

The dilating catheter is passed through the guiding catheter into the coronary artery. The tip of the dilating catheter is passed through the stenotic lesion in the coronary artery. A balloon on the tip of the dilating catheter is then inflated with a fluid. The balloon forces the blockage open and enlarges the lumen, or passage, through the artery.

A problem sometimes develops with this technique, when the dilating catheter has to pass through a tight stenosis or blockage. The reactionary force on the catheter assembly may cause the guiding catheter to slip out of the coronary opening. This results in an unstable condition, and makes it much more difficult to pass the dilating catheter through the stenotic lesion.

The catheter assembly of the invention overcomes this problem by providing an inflatable balloon near the tip of the guiding catheter. After the guiding catheter has been inserted into the opening of the coronary artery, the balloon is inflated. The balloon engages the inner surface of the coronary artery, and stabilizes the guiding catheter. The dilating catheter is then passed through the guiding catheter and through the stenotic lesion, without forcing the guiding catheter out of the coronary lumen.

Side holes in the guiding catheter allow blood to bypass the inflated balloon on the guiding catheter. Otherwise, the inflated balloon would obstruct the flow of blood to the coronary artery.

DESCRIPTION OF THE DRAWINGS

FIG. 1 is a side view of a guiding catheter of the invention, with the tip of the catheter inserted into a coronary lumen.

FIG. 2 is a side view of the catheter assembly of the invention.

FIG. 3 is a side view of the proximal end of the guiding catheter of the invention.

FIG. 4 is a sectional view of the guiding catheter, as seen alonglines 4--4 in FIG. 3.

DESCRIPTION OF THE PREFERRED EMBODIMENT

FIG. 1 shows the guiding catheter 11 of the invention. The guiding catheter 11 has been passed through the femoral artery to theaorta 13. FIG. 1 shows only a section of theaorta 13, theaortic valve 15, the right maincoronary artery 17, and the left maincoronary artery 19.

Thetip 21 of the guiding catheter 11 is shown inserted into the opening, orostium 23, of the left maincoronary artery 19. Other guiding catheters may be shaped differently, for insertion elsewhere, such as into the right maincoronary artery 17 or into theaortic valve 15. The left coronary guiding catheter 11, shown in FIG. 1, is shown merely as an example.

The guiding catheter 11 has aninflatable balloon 25 near thetip 21. In FIG. 1, theballoon 25 is deflated.

The guiding catheter 11 also has aside hole 27 above theballoon 25. Theside hole 27 passes through the guiding catheter 11 to allow blood to flow from theaorta 13, through theside hole 27, and out thetip 21 of the guiding catheter 11.

In FIG. 2, theballoon 25 of the guiding catheter 11 is shown inflated. When theballoon 25 is inflated, theballoon 25 engages the inner surface of the coronary lumen of the left maincoronary artery 19.

FIG. 2 also shows thedilating catheter 29, which extends through the guiding catheter 11 and out into the left maincoronary artery 19. The dilatingcatheter 29 has been passed along aguide wire 30 through a stenotic lesion 31 on the inner surface of the left maincoronary artery 19. Aninflatable balloon 33 of the dilatingcatheter 29 has been positioned within the stenotic lesion 31.

The proximal end of the guiding catheter 11 is illustrated in FIG. 3. Anadapter body 35 is connected to the proximal end of the guiding catheter 11. Theadapter body 35 is a Y-shaped body, which has twoaccess conduits 37, 39. Access conduit 37 leads to themain lumen 41 of the guiding catheter 11, shown in FIG. 4. Themain lumen 41 of the guiding catheter 11 is the conduit through which the dilatingcatheter 29 is passed.

Thesecond access conduit 39 leads to asmall side lumen 43 in the guiding catheter 11. Normal saline solution, or a mixture of water and radiopaque material, may be injected through thesecond access conduit 39 and theside lumen 43 to inflate theballoon 25 on the guiding catheter 11. The saline solution or radiopaque material may also be removed through theaccess conduit 39 to deflate theballoon 25 on the guiding catheter 11.

The catheter assembly of the invention is used in a method of performing percutaneous transluminal coronary angioplasty. The guiding catheter 11 is inserted through the femoral artery into theaorta 13. Thetip 21 of the guiding catheter 11 is inserted into theostium 23 of the left maincoronary artery 19.

Saline solution or radiopaque material is then injected through theaccess conduit 39 to inflate theballoon 25 on the guiding catheter 11. Theballoon 25 is inflated until it engages the inner surface of thecoronary lumen 19. The engagement between theballoon 25 on the guiding catheter 11 and theostium 23 of the maincoronary artery 19 locks the guiding catheter 11 in place.

Blood is perfused through theside hole 27 and thetip 21 of the guiding catheter 11 into the maincoronary artery 19. Blood flow is thus not restricted by the inflatedballoon 25 on the guiding catheter 11.

The dilatingcatheter 29 is then passed through the guiding catheter 11 until theballoon 33 on the dilatingcatheter 29 passes through the stenotic lesion 31 in thecoronary artery 19. Saline solution is then inserted through the lumen of the dilatingcatheter 29 to inflate theballoon 33 on the dilatingcatheter 29. Theballoon 33 on thedilating catheter 29 dilates the lesion 31.

The saline solution is then removed from the dilatingcatheter 29 to deflate theballoon 33. The dilatingcatheter 29 is then removed from the area of the lesion 31. If the dilatingcatheter 29 needs to be repositioned, theballoon 25 on the guiding catheter 11 can be reinflated to hold the guiding catheter 11 in place.

The catheter assembly of the invention and the method of using the catheter assembly have an advantage over the assemblies and methods of the prior art. Theballoon 25 on the guiding catheter 11 holds thetip 21 of the guiding catheter 11 in theostium 23 of thecoronary artery 19. This holds the guiding catheter 11 in place, allowing the dilatingcatheter 29 to be passed through tight stenotic lesions 31 more easily. Further, although theballoon 25 on the guiding catheter 11 contacts the inner surface of thecoronary artery 19, blood flow is not restricted. Blood is perfused through theside hole 27 in the guiding catheter 11.

Only the preferred embodiment of the invention has been illustrated. It should be understood that the invention is not limited to the embodiment disclosed, but is capable of numerous rearrangements, modifications, and substitutions of parts and elements without departing from the spirit of the invention.

Claims

I claim:

1. A catheter assembly for performing percutaneous transluminal coronary angioplasty, said assembly comprising:

a dilating catheter having proximate and distal ends;

a dilating balloon, said dilating balloon being formed at the distal end of said dilating catheter;

means for inflating said dilating balloon;

a guide catheter having proximate and distal ends, said guide catheter defining a first lumen having a hollow open tip at the distal end thereof, a second lumen, and an aperture formed in the wall of said catheter adjacent the distal end of said catheter, said aperture communicating with said first lumen and said hollow tip to form a blood perfusion channel, said first lumen having a diameter sufficient to slidably receive said dilation catheter while simultaneously allowing blood to perfuse around said dilation catheter to an arterial area between said hollow tip and said dilation balloon;

a stabilizing balloon formed at the distal end of said guide catheter located between said aperture and said distal hollow tip, said stabilizing balloon being adapted to engage the walls of the coronary artery when inflated with sufficient force to stabilize said dilating catheter and dilating balloon when said dilating balloon is inflated, said second lumen communicating with said stabilizing balloon to provide means for inflating said stabilizing balloon.

2. The catheter assembly of claim 1 wherein a plurality of apertures communicate with said first lumen and hollow tip to form blood perfusion means.

3. The catheter assembly of claim 1 wherein said assembly further comprises a Y-shaped body, said body defining access channels to provide access to said second lumen and said dilating catheter.

4. The catheter assembly of claim 1 wherein said guide balloon and said dilating balloon may be repeatedly inflated and deflated.

5. The catheter assembly of claim 1 wherein fluid containing a radiopaque material is used to inflate said guide balloon.

6. The catheter assembly of claim 1 wherein fluid containing radiopaque material is used to inflate said dilating balloon.